These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
201 related articles for article (PubMed ID: 27626395)
1. Synthesis and Biological Evaluation of Triazolyl 13α-Estrone-Nucleoside Bioconjugates. Bodnár B; Mernyák E; Wölfling J; Schneider G; Herman BE; Szécsi M; Sinka I; Zupkó I; Kupihár Z; Kovács L Molecules; 2016 Sep; 21(9):. PubMed ID: 27626395 [TBL] [Abstract][Full Text] [Related]
2. Synthesis and biological evaluation of 13α-estrone derivatives as potential antiproliferative agents. Szabó J; Pataki Z; Wölfling J; Schneider G; Bózsity N; Minorics R; Zupkó I; Mernyák E Steroids; 2016 Sep; 113():14-21. PubMed ID: 27263437 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and in vitro pharmacological evaluation of N-[(1-benzyl-1,2,3-triazol-4-yl)methyl]-carboxamides on d-secoestrone scaffolds. Szabó J; Bacsa I; Wölfling J; Schneider G; Zupkó I; Varga M; Herman BE; Kalmár L; Szécsi M; Mernyák E J Enzyme Inhib Med Chem; 2016 Aug; 31(4):574-9. PubMed ID: 26360618 [TBL] [Abstract][Full Text] [Related]
4. Synthesis and in vitro antiproliferative evaluation of d-secooxime derivatives of 13β- and 13α-estrone. Mernyák E; Fiser G; Szabó J; Bodnár B; Schneider G; Kovács I; Ocsovszki I; Zupkó I; Wölfling J Steroids; 2014 Nov; 89():47-55. PubMed ID: 25150017 [TBL] [Abstract][Full Text] [Related]
5. Synthesis of trans-16-triazolyl-13α-methyl-17-estradiol diastereomers and the effects of structural modifications on their in vitro antiproliferative activities. Mernyák E; Kovács I; Minorics R; Sere P; Czégány D; Sinka I; Wölfling J; Schneider G; Újfaludi Z; Boros I; Ocsovszki I; Varga M; Zupkó I J Steroid Biochem Mol Biol; 2015 Jun; 150():123-34. PubMed ID: 25845933 [TBL] [Abstract][Full Text] [Related]
6. Synthesis and in vitro investigation of potential antiproliferative monosaccharide-d-secoestrone bioconjugates. Bodnár B; Mernyák E; Szabó J; Wölfling J; Schneider G; Zupkó I; Kupihár Z; Kovács L Bioorg Med Chem Lett; 2017 May; 27(9):1938-1942. PubMed ID: 28343874 [TBL] [Abstract][Full Text] [Related]
7. Comparative investigation of the in vitro inhibitory potencies of 13-epimeric estrones and D-secoestrones towards 17β-hydroxysteroid dehydrogenase type 1. Herman BE; Szabó J; Bacsa I; Wölfling J; Schneider G; Bálint M; Hetényi C; Mernyák E; Szécsi M J Enzyme Inhib Med Chem; 2016; 31(sup3):61-69. PubMed ID: 27424610 [TBL] [Abstract][Full Text] [Related]
8. Direct antiproliferative effect of nonsteroidal 17β-hydroxysteroid dehydrogenase type 1 inhibitors in vitro. Berényi Á; Frotscher M; Marchais-Oberwinkler S; Hartmann RW; Minorics R; Ocsovszki I; Falkay G; Zupkó I J Enzyme Inhib Med Chem; 2013 Aug; 28(4):695-703. PubMed ID: 22471733 [TBL] [Abstract][Full Text] [Related]
9. Synthesis of Estrone Heterodimers and Evaluation of Their In Vitro Antiproliferative Activity. Bózsity N; Nagy V; Szabó J; Pálházi B; Kele Z; Resch V; Paragi G; Zupkó I; Minorics R; Mernyák E Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38673860 [TBL] [Abstract][Full Text] [Related]
10. Nucleoside dimers analogs containing floxuridine and thymidine with unnatural linker groups: synthesis and cancer line studies. Part III. Baraniak D; Ruszkowski P; Baranowski D; Framski G; Boryski J Nucleosides Nucleotides Nucleic Acids; 2019; 38(12):980-1005. PubMed ID: 31380708 [TBL] [Abstract][Full Text] [Related]
11. Synthesis of A-ring halogenated 13α-estrone derivatives as potential 17β-HSD1 inhibitors. Bacsa I; Jójárt R; Schneider G; Wölfling J; Maróti P; Herman BE; Szécsi M; Mernyák E Steroids; 2015 Dec; 104():230-6. PubMed ID: 26476182 [TBL] [Abstract][Full Text] [Related]
12. Synthesis and in Vitro Antiproliferative Evaluation of C-13 Epimers of Triazolyl-d-Secoestrone Alcohols: The First Potent 13α-d-Secoestrone Derivative. Szabó J; Jerkovics N; Schneider G; Wölfling J; Bózsity N; Minorics R; Zupkó I; Mernyák E Molecules; 2016 May; 21(5):. PubMed ID: 27187336 [TBL] [Abstract][Full Text] [Related]
14. Estradiol and estrone C-16 derivatives as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: blocking of ER+ breast cancer cell proliferation induced by estrone. Laplante Y; Cadot C; Fournier MA; Poirier D Bioorg Med Chem; 2008 Feb; 16(4):1849-60. PubMed ID: 18035543 [TBL] [Abstract][Full Text] [Related]
15. Synthesis of novel 13α-estrone derivatives by Sonogashira coupling as potential 17β-HSD1 inhibitors. Bacsa I; Jójárt R; Wölfling J; Schneider G; Herman BE; Szécsi M; Mernyák E Beilstein J Org Chem; 2017; 13():1303-1309. PubMed ID: 28694873 [TBL] [Abstract][Full Text] [Related]
16. Synthesis of substituted 15β-alkoxy estrone derivatives and their cofactor-dependent inhibitory effect on 17β-HSD1. Herman BE; Kiss A; Wölfling J; Mernyák E; Szécsi M; Schneider G J Enzyme Inhib Med Chem; 2019 Dec; 34(1):1271-1286. PubMed ID: 31307240 [TBL] [Abstract][Full Text] [Related]
17. Stereoselective synthesis of the four 16-hydroxymethyl-3-methoxy- and 16-hydroxymethyl-3-benzyloxy-13α-estra-1,3,5(10)-trien-17-ol isomers and their antiproliferative activities. Kiss A; Mernyák E; Wölfling J; Sinka I; Zupkó I; Schneider G Steroids; 2018 Jun; 134():67-77. PubMed ID: 29501755 [TBL] [Abstract][Full Text] [Related]
18. Synthesis and Antiproliferative Activity of Steroidal Diaryl Ethers. Kovács É; Ali H; Minorics R; Traj P; Resch V; Paragi G; Bruszel B; Zupkó I; Mernyák E Molecules; 2023 Jan; 28(3):. PubMed ID: 36770863 [TBL] [Abstract][Full Text] [Related]
19. A facile 'click' approach to novel 15β-triazolyl-5α-androstane derivatives, and an evaluation of their antiproliferative activities in vitro. Kádár Z; Molnár J; Schneider G; Zupkó I; Frank É Bioorg Med Chem; 2012 Feb; 20(4):1396-402. PubMed ID: 22277592 [TBL] [Abstract][Full Text] [Related]
20. Synthesis and structure-activity relationships of 2- and/or 4-halogenated 13β- and 13α-estrone derivatives as enzyme inhibitors of estrogen biosynthesis. Bacsa I; Herman BE; Jójárt R; Herman KS; Wölfling J; Schneider G; Varga M; Tömböly C; Rižner TL; Szécsi M; Mernyák E J Enzyme Inhib Med Chem; 2018 Dec; 33(1):1271-1282. PubMed ID: 30230387 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]